| | | Single nucleotide variant (missense variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions | |
| | | Single nucleotide variant (missense variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +1 more | |
| | | Single nucleotide variant (missense variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +1 more | |
| | | Single nucleotide variant (missense variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Deletion | not specified | |
| | | Single nucleotide variant (synonymous variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +1 more | |
| | GRN, LOC125177489 (T238fs) | Deletion (frameshift variant) | Neuronal ceroid lipofuscinosis 11 +1 more | |
| | | Single nucleotide variant (missense variant) | Neuronal ceroid lipofuscinosis 11 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Neuronal ceroid lipofuscinosis 11 +1 more | |
| | | Single nucleotide variant (missense variant) | Neuronal ceroid lipofuscinosis 11 +2 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +1 more | |
| | | Single nucleotide variant (intron variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +1 more | |
| | | Duplication (splice donor variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +1 more | |
| | | Single nucleotide variant (missense variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Microsatellite (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Neuronal ceroid lipofuscinosis 11 | |
| | | Single nucleotide variant (intron variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (splice acceptor variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (synonymous variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Protein only | Frontotemporal dementia | |
| | | Microsatellite (splice donor variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | | Single nucleotide variant (splice donor variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Duplication (frameshift variant) | not provided | |
| | | Microsatellite (frameshift variant) | not provided | |
| | | Microsatellite (frameshift variant) | not provided | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Insertion (frameshift variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Insertion (splice donor variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +2 more | |
| | | Single nucleotide variant (splice donor variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +1 more | |
| | | Single nucleotide variant (synonymous variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (splice acceptor variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Duplication (frameshift variant) | not provided | |
| | | Insertion (frameshift variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (splice acceptor variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions | |